Variants in gene ZNF862 - ClinVar Miner

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
1	1	132	13	2	148

Condition and significance breakdown #

Total conditions: 5

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
not specified	0	0	132	11	0	143
not provided	0	0	0	1	2	3
Fibromatosis, gingival, 6	1	0	0	0	0	1
Gingival fibromatosis	0	1	0	0	0	1
Long QT syndrome	0	0	0	1	0	1

Submitter and significance breakdown #

Total submitters: 7

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Ambry Genetics	0	0	132	11	0	143
Labcorp Genetics (formerly Invitae), Labcorp	0	0	0	0	2	2
Breakthrough Genomics, Breakthrough Genomics	0	0	0	0	2	2
OMIM	1	0	0	0	0	1
Medical Research Institute, Tokyo Medical and Dental University	0	0	0	1	0	1
CeGaT Center for Human Genetics Tuebingen	0	0	0	1	0	1
Clinical Research Group, BGI genomics	0	1	0	0	0	1

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